Canonical Allele Identifier: PA2828325186
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577621
ClinVar RCV Id: RCV003324958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala88Gly
CA415173787
NM_001369391.2:c.263C>G